College of Polymer Science and Engineering, Sichuan University, Yi Huan Road, South Section One, No. 24, Chengdu 610065, People's Republic of China.
Acta Biomater. 2012 Dec;8(12):4380-8. doi: 10.1016/j.actbio.2012.08.014. Epub 2012 Aug 16.
Insulin, glucose oxidase and positively charged star polymers were incorporated into multilayer films by the layer-by-layer (LbL) assembly method. It is interesting to find that the arrangement sequence of the three components could significantly affect the glucose-responsive controlled release behaviors. The insulin release in vitro could be tuned to linear release and obtain desired "on-off" sensitivity in response to stepwise glucose challenge, just by rearranging the assembly sequence of LbL building blocks. Further, the controlled release of insulin in vivo, as well as the hypoglycemic effect, could be obviously prolonged from 17days to 36days by this simple strategy without changing the dosage of all the LbL components. In addition to provide a potential glucose-responsive delivery system for insulin, the strategy described in this paper could be valuable for various drug-incorporated LbL systems with three or more components.
胰岛素、葡萄糖氧化酶和带正电荷的星形聚合物通过层层(LbL)组装方法被纳入多层膜中。有趣的是,发现这三种成分的排列顺序会显著影响葡萄糖响应的控制释放行为。通过重新排列 LbL 构建块的组装顺序,体外胰岛素的释放可以调制成线性释放,并对逐步葡萄糖挑战获得所需的“开-关”灵敏度。此外,通过这种简单的策略,无需改变所有 LbL 成分的剂量,体内胰岛素的控制释放以及降血糖效果可以从 17 天明显延长至 36 天。除了为胰岛素提供潜在的葡萄糖响应递送系统外,本文中描述的策略对于具有三个或更多成分的各种药物掺入 LbL 系统可能具有重要价值。